Variant #0000613998 (NC_000012.11:g.21623300del, NC_000012.11(NM_002907.3):c.1798-5del (RECQL))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.21623300del
DNA change (hg38) g.21470366del
Published as RECQL(NM_002907.3):c.1798-5delT (p.?), RECQL(NM_002907.4):c.1798-5delT
ISCN -
DB-ID PYROXD1_000021 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RECQL NM_002907.3 -/. - c.1798-5del r.spl? p.?
PYROXD1 NM_024854.3 -/. - c.*1612del r.(?) p.(=)


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